Lee D J, Abeyratne A, Carson D A, Corr M
Department of Medicine and The Sam and Rose Stein Institute for Research on Aging, University of California, San Diego, La Jolla, California 92093-0663, USA.
J Exp Med. 1998 Feb 2;187(3):433-8. doi: 10.1084/jem.187.3.433.
The majority of T cell responses are restricted to peptide antigens bound by polymorphic major histocompatibility complex (MHC) molecules. However, peptide antigens can be presented to T cells by murine non-MHC-encoded CD1d (mCD1) molecules, and human T cell lines specific for nonpeptide antigens presented on CD1 isoforms have been identified. It is shown here that antigen-specific, mCD1-restricted lymphocytes can be generated in vivo by immunizing mice with a combination of plasmids encoding chicken ovalbumin, murine CD1d, and costimulatory molecules. Splenocytes from immunized mice have CD1d-restricted, MHC- unrestricted, ovalbumin-specific cytolytic activity that can be inhibited by anti-CD1 antibodies as well as a competing CD1-binding peptide. These results suggest a physiologic role for murine CD1d to present exogenous protein antigens.
大多数T细胞反应局限于由多态性主要组织相容性复合体(MHC)分子结合的肽抗原。然而,肽抗原可由小鼠非MHC编码的CD1d(mCD1)分子呈递给T细胞,并且已经鉴定出对CD1同种型上呈递的非肽抗原具有特异性的人T细胞系。本文表明,通过用编码鸡卵清蛋白、小鼠CD1d和共刺激分子的质粒组合免疫小鼠,可在体内产生抗原特异性、mCD1限制的淋巴细胞。免疫小鼠的脾细胞具有CD1d限制、MHC非限制、卵清蛋白特异性的细胞溶解活性,该活性可被抗CD1抗体以及竞争性CD1结合肽抑制。这些结果表明小鼠CD1d在呈递外源性蛋白质抗原方面具有生理作用。